chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145341702145341704GA55GENIChomozygous128087959
4145341851145341852GA66GENIChomozygous112870784
4145342547145342547AC55GENICpossibly homozygous128087960
4145342744145342745TA50GENIChomozygous112870785
4145343247145343248GA52GENIChomozygous112870786
4145343659145343660CT39GENIChomozygous112870787
4145344906145344914ACACACAG39GENIChomozygous128087962
4145345010145345011TC60GENIChomozygous112870788
4145347173145347174CT45GENIChomozygous112870789
4145348770145348771CA26GENIChomozygous112870792
4145349663145349664GA62GENIChomozygous112870796
4145350121145350122AT47GENIChomozygous112870797
4145350671145350672CT45GENIChomozygous112870798
4145351090145351091CT43GENIChomozygous112870799
4145352309145352309G57GENIChomozygous128087964
4145352472145352473G67GENIChomozygous128087965
4145354146145354147GC59GENIChomozygous112870800
4145354549145354550GA45GENIChomozygous112870801
4145354613145354615TG20GENIChomozygous128087966
4145354894145354895CT39GENIChomozygous112870803
4145356424145356425GA39GENIChomozygous112870807
4145355614145355615AG48GENIChomozygous112870804
4145356361145356362AC36GENIChomozygous112870805
4145356418145356419TC36GENIChomozygous112870806
4145356960145356961AT52GENIChomozygous112870808
4145357076145357077TC39GENIChomozygous112870809
4145357179145357180GC51GENIChomozygous112870810
4145357227145357227T39GENIChomozygous128087967
4145357360145357361TA43GENIChomozygous112870811
4145358592145358593CT38GENIChomozygous112870812
4145358919145358920TC45GENIChomozygous112870813
4145359534145359535AG51GENIChomozygous112870814
4145359628145359629TG52GENIChomozygous112870815
4145361065145361066AG49GENIChomozygous112870816
4145361458145361460AG20GENICheterozygous129904596
4145362996145362997CT36GENIChomozygous112870817
4145363773145363774CT43GENIChomozygous112870818
4145364439145364440TC51GENIChomozygous112870819
4145364702145364703CT47GENIChomozygous112870820